Degradation of 1H-benzotriazole using vacuum ultraviolet: a prospective treatment method for micro-pollutants

被引:6
|
作者
Ye, Jinshao [1 ,2 ]
Hu, Han [1 ]
Chen, Ya [1 ]
Chen, Yujia [1 ]
Ou, Huase [1 ]
机构
[1] Jinan Univ, Sch Environm, Guangdong Key Lab Environm Pollut & Hlth, Guangzhou 510632, Guangdong, Peoples R China
[2] Lawrence Berkeley Natl Lab, Joint Genome Inst, Walnut Creek, CA 94598 USA
基金
中国国家自然科学基金;
关键词
advanced oxidation technologies; corrosion inhibitor; kinetics; radical reaction; toxicology; 185; NM; WATER-TREATMENT; KINETIC-MODEL; BISPHENOL-A; UV; OXIDATION; BENZOTRIAZOLE; PHOTODEGRADATION; MICROPOLLUTANTS; REMOVAL;
D O I
10.2166/wst.2019.320
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Benzotriazoles (BTs) attract increasing concerns because of abundant presence in environmental water bodies. In this study, degradation of 1H-benzotriazole (1H-BT) was performed by a customized vacuum ultraviolet (VUV) device emitting 185 + 254 nm (VUV/UV-C) irradiation. Degradation of 1H-BT presented an apparent rate constant reached 8.17 x 10(-4) s(-1). Degradation mechanisms included 185 + 254 nm photodegradation and radical reaction. The later one may be the predominant one, which presented a k(center dot OH-1H-BT) at (7.3 +/- 0.8) x 10(9) M-1 s(-1). Effects of anions revealed that VUV interception and radical trapping were the dominant restraining factors. Degradation of 1H-BT can be attributed to VUV induced radical-based oxidation. Radical-induced addition, substitution and fracture generated abundant hydroxylated and open-loop products during 10-45 min. Identification using reactive oxygen species and apoptosis in Escherichia coli was conducted. Variations of these two indicators revealed that the incomplete degradation products presented higher toxicities than 1H-BT, and a further mineralization reduced their toxicities. In the pure water solution with little impurities, VUV can induce efficient degradation of 1H-BT, suggesting its potential for eliminating and detoxifying MPs.
引用
收藏
页码:773 / 783
页数:11
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